Sandra Peacock
Impact in
-
- Prenatal Screening and Diagnostics
- Fetal and Pediatric Neurological Disorders
- Genetics top 10%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
Papers in
-
- Prenatal Screening and Diagnostics 5
- Fetal and Pediatric Neurological Disorders 1
- Genetics 5
- Genomic variations and chromosomal abnormalities 4
- Genetics and Neurodevelopmental Disorders 3
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 1
- Genomics and Rare Diseases 1
- Co-authors
- Sau Wai Cheung (5 shared papers)Janice Smith (2 shared papers)Amy M. Breman (2 shared papers)Ignatia B. Van den Veyver (2 shared papers)Weimin Bi (1 shared paper)Alicia Braxton (1 shared paper)Andrea Petersen (1 shared paper)Patricia A. Ward (1 shared paper)
- Journals
- American Journal of Obstetrics and Gynecology (2 papers)Clinical Genetics (1 paper)The Journal of Urology (1 paper)Prenatal Diagnosis (1 paper)Molecular Cytogenetics (1 paper)
- Partner nations
- United StatesBrazil
In The Last Decade
Sandra Peacock
11 papers receiving 493 citations
Peers
Comparison fields: 5 of 50
- Pediatrics, Perinatology and Child Health 189
- Genetics 255
- Reproductive Medicine 26
- Developmental Biology 5
- Molecular Biology 141
Countries citing papers authored by Sandra Peacock
This map shows the geographic impact of Sandra Peacock's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Sandra Peacock with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Sandra Peacock more than expected).
Fields of papers citing papers by Sandra Peacock
This network shows the impact of papers produced by Sandra Peacock. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Sandra Peacock. The network helps show where Sandra Peacock may publish in the future.
Co-authors
The 25 scholars most cited alongside Sandra Peacock, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2009 | 146 | |
| 2 | 2017 | 128 | |
| 3 | 2009 | 50 | |
| 4 | 2021 | 47 | |
| 5 | 2010 | 46 | |
| 6 | 2014 | 33 | |
| 7 | 2015 | 23 | |
| 8 | 2018 | 13 | |
| 9 | 2008 | 11 | |
| 10 | 2011 | 1 | |
| 11 | 2018 | 1 |
About Sandra Peacock
Sandra Peacock is a scholar working on Pediatrics, Perinatology and Child Health, Genetics, Plant Science, Pulmonary and Respiratory Medicine and Infectious Diseases, having authored 11 papers that have together received 499 indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (5 papers), Genomic variations and chromosomal abnormalities (4 papers), Genetics and Neurodevelopmental Disorders (3 papers), Chromosomal and Genetic Variations (3 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (1 paper), Genomics and Rare Diseases (1 paper), Fetal and Pediatric Neurological Disorders (1 paper) and Cystic Fibrosis Research Advances (1 paper). The work is most often cited by research in Pediatrics, Perinatology and Child Health (189 citations), Genetics (255 citations), Reproductive Medicine (26 citations), Developmental Biology (5 citations) and Molecular Biology (141 citations). Sandra Peacock has collaborated with scholars based in United States and Brazil. Frequent co-authors include Sau Wai Cheung, Janice Smith, Amy M. Breman, Ignatia B. Van den Veyver, Weimin Bi, Alicia Braxton, Andrea Petersen, Patricia A. Ward, Ankita Patel and Paweł Stankiewicz. Their work appears in journals such as American Journal of Obstetrics and Gynecology, Clinical Genetics, The Journal of Urology, Prenatal Diagnosis and Molecular Cytogenetics.
Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.